ENST00000683929.1:c.*255C>T
(WWOX)
|
ENSP00000507689.1:n.*255C>T
|
|
ENST00000566780.6:c.1141C>T
(WWOX)
MANE Select
|
ENSP00000457230.1:p.Arg381Cys
|
|
ENST00000402655.6:c.494C>T
(WWOX)
|
ENSP00000384238.2:p.Pro165Leu
|
|
ENST00000406884.6:c.601C>T
(WWOX)
|
ENSP00000384495.2:p.Arg201Cys
|
|
ENST00000539474.6:c.570C>T
(WWOX)
|
ENSP00000445210.2:p.Ala190=
|
|
ENST00000566103.1:n.208C>T
(WWOX)
|
|
|
ENST00000566780.5:c.1141C>T
(WWOX)
|
ENSP00000457230.1:p.Arg381Cys
|
|
ENST00000569332.5:c.*938C>T
(WWOX)
|
ENSP00000454788.1:n.*938C>T
|
|
NM_001291997.1:c.802C>T
(WWOX)
|
NP_001278926.1:p.Arg268Cys
|
|
NM_016373.3:c.1141C>T
(WWOX)
|
NP_057457.1:p.Arg381Cys
|
|
XM_011523100.1:c.1237C>T
(WWOX)
|
XP_011521402.1:p.Arg413Cys
|
|
XM_011523103.3:c.*113C>T
(WWOX)
|
XP_011521405.1:n.*113C>T
|
|
XM_017023279.1:c.227C>T
(WWOX)
|
XP_016878768.1:p.Pro76Leu
|
|
XM_024450279.1:c.*1238G>A
(MAF)
|
XP_024306047.1:n.*1238G>A
|
|
XR_001751902.2:n.4440G>A
(MAF)
|
|
|
XR_002957802.1:n.4440G>A
(MAF)
|
|
|
XR_002957803.1:n.4440G>A
(MAF)
|
|
|
XR_002957804.1:n.4440G>A
(MAF)
|
|
|
NM_016373.4:c.1141C>T
(WWOX)
MANE Select
|
NP_057457.1:p.Arg381Cys
|
|
NM_001291997.2:c.802C>T
(WWOX)
|
NP_001278926.1:p.Arg268Cys
|
|